A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029805



Internal ID20596845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57786392..57787473hg38UCSC Ensembl
chr16:57820304..57821385hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507319
Supporting Variants
Samples
Known GenesKIFC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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